{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99817",
      "recalling_firm": "Canon Medical System, USA, INC.",
      "address_1": "2441 Michelle Dr",
      "address_2": "N/A",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of ID.",
      "recall_number": "Z-0108-2027",
      "product_description": "Alphenix INFX-8000C/B5",
      "product_quantity": "1 unit",
      "reason_for_recall": "Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error",
      "recall_initiation_date": "20260826",
      "center_classification_date": "20261007",
      "report_date": "20261014",
      "code_info": "Serial no. B5F2532011/UDI: 4987670100192"
    }
  ]
}